3989-00-2

Usage

Uses

2-(2-THIENYLSULFONYL)THIOPHENE is used as a chemical intermediate in the synthesis of various organic compounds and pharmaceuticals. Its unique structure and reactivity make it a valuable building block for the development of new molecules with potential applications in various industries.
Used in Pharmaceutical Industry:
2-(2-THIENYLSULFONYL)THIOPHENE is used as a key intermediate in the synthesis of drug candidates for the treatment of various diseases. Its ability to form stable bonds with other molecules allows for the creation of new compounds with improved pharmacological properties.
Used in Chemical Research:
2-(2-THIENYLSULFONYL)THIOPHENE is used as a research tool in the field of organic chemistry to study the reactivity and properties of thiophene-based compounds. It can be employed in various chemical reactions to gain insights into the behavior of similar molecules and to develop new synthetic methods.
Used in Material Science:
2-(2-THIENYLSULFONYL)THIOPHENE can be used in the development of new materials with unique properties, such as conductive polymers or organic semiconductors. Its incorporation into these materials can lead to improved performance and new applications in areas like electronics, sensors, and energy storage.

Upstream product

• 3988-99-6 bis(thien-2-yl)sulfide 
• 188290-36-0 thiophene 
• 38945-01-6 sodium thiophene-2-sulphinate 

Relevant academic research and scientific papers

Facile synthesis of diarylsulfones from arenes and 3CdSO4·xH2O via mechanochemistry

A variety of substituted diarylsulfones could be synthesized by simple arenes and 3CdSO4·xH2O in the presence of P2O5 under high-speed ball milling. It was suggest the aromatic sulfonation was performed by arene and in situ generated H2SO4, following-up by electrophilic substitution with another arene to give diarylsulfone.

Synthesis of symmetrical diaryl sulfone by homocoupling of sodium arylsulfinate

An efficient practical homocoupling reaction of sodium arylsulfinate promoted by Cu(II) is reported whereby symmetrical diaryl sulfone derivatives are obtained with high selectivity and reactivity by intermolecular cross-coupling. This homocoupling reacti

The development of catalytic oxovanadium(IV)-containing microspheres for the oxidation of various organosulfur compounds

The development of poly[allylSB-co-EGDMA] beads containing a tetradentate ligand was achieved via suspension polymerization. The catalyst poly[allylSB-co-EGDMA]-VO was synthesized by reacting VIVOSO 4 with poly[allylSB-co-EGDMA]. XPS

Synthesis of symmetric diaryl sulfones with dimethyl sulfate

In this procedure dimethyl sulfate was used for preparation of symmetric diaryl sulfones. First, dimethyl sulfate was treated with pyridine, then activated by Tf2O to generate SO2 as the functional group for synthesis of diaryl sulfones. It is noticeable that this reaction was carried out in moderate conditions and products obtained in short times and good yields.